Title |
Ajulemic acid (IP-751): Synthesis, proof of principle, toxicity studies, and clinical trials
|
---|---|
Published in |
The AAPS Journal, June 2005
|
DOI | 10.1208/aapsj070115 |
Pubmed ID | |
Authors |
Summer Burstein |
Abstract |
Ajulemic acid (CT-3, IP-751, 1',1'-dimethylheptyl-Delta8-tetrahydrocannabinol-11-oic acid) (AJA) has a cannabinoid-derived structure; however, there is no evidence that it produces psychotropic actions when given at therapeutic doses. In a variety of animal assays, AJA shows efficacy in models for pain and inflammation. Furthermore, in the rat adjuvant arthritis model, it displayed a remarkable action in preventing the destruction of inflamed joints. A phase-2 human trial with chronic, neuropathic pain patients suggested that AJA could become a useful drug for treating this condition. Its low toxicity, particularly its lack of ulcerogenicity, further suggests that it will have a highly favorable therapeutic index and may replace some of the current anti-inflammatory/analgesic medications. Studies to date indicate a unique mechanism of action for AJA that may explain its lack of adverse side effects. |
X Demographics
Geographical breakdown
Country | Count | As % |
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Unknown | 1 | 100% |
Demographic breakdown
Type | Count | As % |
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Members of the public | 1 | 100% |
Mendeley readers
Geographical breakdown
Country | Count | As % |
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United States | 2 | 3% |
Italy | 2 | 3% |
Unknown | 69 | 95% |
Demographic breakdown
Readers by professional status | Count | As % |
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Researcher | 15 | 21% |
Student > Bachelor | 12 | 16% |
Student > Ph. D. Student | 10 | 14% |
Other | 8 | 11% |
Student > Master | 8 | 11% |
Other | 7 | 10% |
Unknown | 13 | 18% |
Readers by discipline | Count | As % |
---|---|---|
Medicine and Dentistry | 22 | 30% |
Agricultural and Biological Sciences | 11 | 15% |
Chemistry | 5 | 7% |
Pharmacology, Toxicology and Pharmaceutical Science | 4 | 5% |
Psychology | 3 | 4% |
Other | 11 | 15% |
Unknown | 17 | 23% |